We reduce risks.
QFINITY Quality Management is a leading business consulting and services firm dedicated to reducing risks and enhancing quality across diverse industries. With a focus on risk-based quality management, quality assurance, GxP compliance, and continuous process improvement, QFINITY supports businesses in optimizing their operations and achieving regulatory excellence.
Located at Wallerfanger Str. 27, Dillingen, Saarland 66763, DE, QFINITY specializes in data quality and integrity, offering professional compliance consulting for pharmaceutical and medical technology companies. The company provides comprehensive support to start-ups, SMEs, and global corporations throughout the entire product lifecycle, ensuring integrated quality management that aligns with essential control objectives.
QFINITY Quality Management is committed to identifying and evaluating process risks, collaborating with clients to implement effective measures that meet official, regulatory, and company requirements. QFINITY consistently expands its range of services to support companies of all sizes. We invite the manager of QFINITY Quality Management to create a customized and exclusive company showcase and product listing on our platform.
Compare QFINITY Quality Management with 3 companies in Business-Consulting-and-Services
| Comparison Field |
QFINITY Quality Managemen...Main Company |
HEISView Profile |
TriEdge BlogView Profile |
ClinProve - CROView Profile |
|---|---|---|---|---|
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Founded Year
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— | 2011 | 2008 | 2020 |
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Company Size
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— | 2-10 | 1 employee | 11-50 |
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City
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Dillingen, Saarland | Freiburg im Breisgau, Baden-Württemberg | Camarillo, CA | Cairo, Egypt |
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Country
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Germany | United States | Egypt | |
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Skills & Keywords
Comparing with main company
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32 Total Skills
Quality Management
GxP Compliance
Risk Management
Data Integrity
Business Consulting
Process Improvement
Regulatory Compliance
Data Governance
Validation of Computerized Systems
Clinical Trials
Process Management
GMP
Consulting
Training
Business Process Management
Validation
GxP
GDP
Qualification
GLP
Supplier Audits
eTMF
Quality Assurance
GCP
Project Management
Site Audits
Risk Based Approach
Computerized Systems
Data Quality
Data Reliability
Raw Data
Source Data
|
14 Total
14 Unique
Unique Skills:
Analysis
Consultation
Development
DHF
EU MDR 2017
FDA 21 CFR 820
+8
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24 Total
24 Unique
Unique Skills:
21 CFR Part 11
Adverse Events
Bioinformatics Cloud Computing
Biotechnology & Pharma
Business process outsourcing
CDER
+18
|
6 Total
6 Unique
Unique Skills:
Biopharmaceuticals
Biostatistics
Clinical Research
Medical Writing
Pharmacovigilance
Process Validation
|
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